Transducer S8-3tRecalls & reported problems across all models
Philips Ultrasound LLC · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one Transducer S8-3t model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 27
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 2
We found 2 models of Transducer S8-3t by Philips Ultrasound LLC in the FDA's device registry (GUDID). Together they are named in 27 adverse event reports in the FDA's MAUDE database, received between Mar 20, 2018 and Feb 5, 2021 — classified as 27 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (18 reports).
2 FDA recall records name at least one of these models by its device identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Transducer S8-3t recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jul 3, 2025Open, Classified
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Z-2398-2025 · Root cause: Device Design · names 2 of these models · Recall details · FDA record ↗
- May 28, 2025Open, Classified
Ultrasound transducer devices were refurbished beyond their useful life.
Z-2061-2025 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗
Most reported Transducer S8-3t problems
Device problems
- Poor Quality Image18
- Image Display Error/Artifact2
- Mechanical Jam2
- No Display/Image2
- Defective Component1
- Device Displays Incorrect Message1
- Display Difficult to Read1
- Mechanical Problem1
Patient problems
- No Consequences Or Impact To Patient14
- No Known Impact Or Consequence To Patient12
- No Clinical Signs, Symptoms or Conditions1
- No Patient Involvement1
Transducer S8-3t models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Transducer S8-3t 989605431171Transducer, ultrasonic, diagnostic2 recalls17 reports
- Transducer S8-3t 989605420183System, imaging, pulsed doppler, ultrasonic2 recalls10 reports
Recent Transducer S8-3t adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionFeb 5, 2021Mechanical Jam; Mechanical Jam
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER HAD AN ARTICULATION ISSUE DURING USE. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 11285673 ↗MalfunctionNov 20, 2020Mechanical Problem; Mechanical Jam; No Apparent Adverse Event; Mechanical Problem; Mechanical Jam; No Apparent Adverse Event
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER HAD AN ARTICULATION ISSUE DURING USE. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10876585 ↗MalfunctionAug 11, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10390790 ↗MalfunctionAug 10, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY DURING USE. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10388397 ↗MalfunctionAug 7, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER HAD AN IMAGE QUALITY ISSUE. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10379969 ↗MalfunctionJul 28, 2020Therapeutic or Diagnostic Output Failure
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER HAD AN ARTICULATION ISSUE DURING USE. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10333699 ↗MalfunctionJul 23, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10314218 ↗MalfunctionJul 16, 2020Image Display Error/Artifact
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING IMAGE ARTIFACTS. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10286335 ↗MalfunctionJul 10, 2020No Display/Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING NO IMAGES. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10257672 ↗MalfunctionJun 29, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10209753 ↗MalfunctionJun 29, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10207188 ↗MalfunctionJun 3, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10116392 ↗MalfunctionApr 13, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9955380 ↗MalfunctionMar 18, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9849883 ↗MalfunctionJan 10, 2020Poor Quality Image
A CUSTOMER REPORTED AN S8-3T MODEL TRANSDUCER WAS PRODUCING POOR IMAGE QUALITY. THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9575963 ↗
Other Philips Ultrasound LLC products
- Transducer C5-13 models · 0 reports · 12 recalls
- EPIQ Diagnostic Ultrasound System9 models · 281 reports · 5 recalls
- Transducer X5-13 models · 0 reports · 10 recalls
- EPIQ 7 DIAGNOSTIC ULTRASOUND SYSTEM5 models · 330 reports · 3 recalls
- Transducer C10-3v2 models · 0 reports · 7 recalls
- Transducer X7-2t4 models · 26 reports · 6 recalls
- Transducer C5-210 models · 0 reports · 6 recalls
- Transducer S5-12 models · 0 reports · 6 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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